“NIDEK” Laser Speckle Flowgraphy - Taiwan Registration 7e4608c17768f0b36dfdd97a4b1f34f7
Access comprehensive regulatory information for “NIDEK” Laser Speckle Flowgraphy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e4608c17768f0b36dfdd97a4b1f34f7 and manufactured by NIDEK CO., LTD., HAMACHO PLANT. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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Device Details
Registration Details
7e4608c17768f0b36dfdd97a4b1f34f7
Ministry of Health Medical Device Import No. 033201
DHA05603320109
Product Details
For details, it is Chinese approved copy of the imitation order
M Ophthalmic devices
M1570 fundus mirror
Imported from abroad
Dates and Status
Jan 10, 2020
Jan 10, 2025

